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N/A N=90 Randomized Screening

Mindfulness, Mental Fatigue, Inhibitory Control and Endurance Performance in Athletes

Mental Fatigue

Enrolled (actual)
90
Serious AEs
0.0%
Results posted
Mar 2026
Primary outcome: Primary: Inhibitory Control: Reaction Time — 461.01; 448.68; 444.35; 465.88 millisecond

Study Design & Population

Study type
Interventional
Phase
N/A
Interventions
Mental fatigue condition (Behavioral); Control condition (Behavioral)
Age
Adult · 18+ yrs
Sex
All
Sponsor
National Taiwan Normal University
Primary completion
Oct 2022

Outcome Measures

OutcomeResultp-value
PRIMARY
Inhibitory Control: Reaction Time
461.01; 448.68; 444.35; 465.88; 446.33; 455.91
PRIMARY
Inhibitory Control: Accuracy
89.26; 84.32; 80.04; 89.14; 87.21; 84.16
PRIMARY
Endurance Performance: Time to Exhaustion
807.62; 783.35; 752.94; 819.99; 794.97; 792.62
PRIMARY
Endurance Performance: Maximum Oxygen Consumption
60.77; 61.70; 57.43; 61.39; 60.65; 58.87
PRIMARY
Changes in Neuroelectrical Activities
-1.29; -1.47; -1.18; -0.12; -1.01; -0.89
SECONDARY
Subjective Mental Fatigue
20.93; 26.29; 27.14; 45.26; 48.00; 51.79
SECONDARY
Objective Mental Fatigue: Reaction Time in Stroop Task
636.66; 626.64; 617.74; 587.14; 591.25; 589.76
SECONDARY
Objective Mental Fatigue: Accuracy in Stroop Task
84.18; 86.39; 85.48; 89.95; 90.29; 89.28
SECONDARY
Mood State
0.148; 0.057; 0.116; 0.111; 0.121; 0.375
SECONDARY
Motivation
87.22; 87.57; 85.89; 87.19; 90.91; 86.43

Summary

This study investigated whether trait mindfulness in athletes is associated with impairments in neurocognitive function and endurance performance resulting from mental fatigue.

Eligibility Criteria

Inclusion Criteria

  • Regular sports training at least 4 hours weekly
  • Normal or corrected-to-normal vision
  • Right-handed

Exclusion Criteria

  • Physical limitation or injury in lower limbs before and during the study
  • Diagnosed or self-reported neurological disorders (e.g., epilepsy)
  • Diagnosed or self-reported major psychiatric illness (e.g., major depression, schizophrenia)
View full record on ClinicalTrials.gov →

Data sourced from ClinicalTrials.gov (NCT05466136). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.

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